Drosophila strain carrying bradeion gene(s) transferred thereinto

ABSTRACT

Provided is a special Drosophila strain having a Bradeion gene artificially incorporated therein to exclusively express the gene in the compound eyes and thus to exhibit rough eye. The Drosophila strain has the following properties:  
     (a) a human-derived Bradeion gene has been transferred in the strain to express the human-derived protein Bradeion in the compound eyes from the developmental period;  
     (b) the compound eyes show morphological abnormality due to the expression of Bradeion; and  
     (c) the morphological abnormality occurring in the compound eyes is multiplied according to the number of transferred Bradeion genes.

TECHNICAL FIELD

[0001] The present invention relates to a special Drosophila strain and the use thereof. Specifically, the special Drosophila strain is generated by artificially incorporating a Bradeion gene, which encodes a protein involved in the long-term survival and the maintenance of the neurotransmission of human cranial nerve cells, into Drosophila melanogaster, which is an experimental insect and is essential for genetic and molecular biological analyses, to exclusively express the gene in the insect's compound eyes and thus to develop rough eye.

BACKGROUND ART

[0002] The molecular medicine revolution of the 21st century aims at, as a post-genome project, the construction of a control monitor system suited for individual characteristics by capturing genes and substances that form the basis of disease. Specifically, the system is intended to establish a medical system that is specific to individual gene types through the detection (via diagnosis and gene monitoring) of risk groups from disease groups that are thought to threaten daily social activities based on the concept of “Quality of Life” and include genetic diseases, cancer and neurodegenerative diseases, the finding of the risk genes of these disease groups, and the searching for the sensitivity against therapy (drug and gene therapy). Here, not only cancer, but also many diseases are multi-gene effects and largely depend on environmental factors. Thus, it is impossible to prevent a disease by controlling a single factor. However, it is possible to take measures to control disease through the development of so-called control technology that controls the conditions of an individual with a disease.

[0003] Now based on this concept, in particular control technology to counter the canceration and the immortalization of cells is actively developed at the molecular level. Specifically, in the studies of technology to control cellular life span, signal transduction is often analyzed. Through these studies, various molecular bases involved in cell proliferation, division and canceration have been revealed. The secretary of the Agency of Industrial Science and Technology has already applied for a patent for Bradeion, which is such a factor controlling cellular life span (JP Patent Publication (Kokai) No. 2000-139470, JP Patent Application No. 2000-308650 and U.S. patent application Ser. No. 09/440,936). This patent application has revealed that Bradeion, which is expressed in cancer and particularly expressed only in colon cancer cells or skin cancer, is naturally useful in early diagnosis, and also satisfies various conditions required of a specific inhibitor or a gene therapy target.

[0004] If such a signalling substance is found, only analytical results at the culture cell level can be obtained with conventional techniques. To further develop disease control or gene function control technology, which is an original purpose, the presence of an appropriate organism model is required. Currently, a special genetically-modified animal such as a knockout mouse is used for this purpose.

DISCLOSURE OF THE INVENTION

[0005] However, the generation of knockout mice and transgenic mice involves considerable difficulties. In addition, gene expression is knocked out from the developmental period, so that, for example, the applicable range and successful examples of such mice are limited. Thus, they cannot be said to be organism models that can satisfy broad demands.

[0006] In recent years, the usability of a fruit fly, Drosophila melanogaster, has been much publicized in comparison with that of mammalian models such as mice. Originally, the use of Drosophila was established as an experimental system for transformation by genetic breeding in the field of genetics in a manner similar to those for corn and peas. Recently, it has begun to be shown that a mutation in an individual trait of Drosophila can reflect a human trait better than a mammalian model, depending on the characteristics of the relevant gene group. In particular, Drosophila is highly useful for gene groups involved in the above-described signal transduction, signal transduction system and cellular life span.

[0007] The experimental system using Drosophila involves transferring a human gene involved in the above signal transduction system into the compound eye formation system. Specifically, it limits the expression vector, so that the gene is expressed exclusively in the compound eye formation system (pUAST and the like, see FIGS. 1 to 3). The compound eye formation system of insects normally comprises a large number of the cells involved in the formation, as previously known. During the developmental period, the consistency system acts to fix the cell cycle at GO/GI, so that the same cell cycle is maintained. After the fixation, the cells differentiate into so-called optic nerve cells. That is, this system can also be used for a system for testing a gene function (nerve cell differentiation potency). Reasons why biofunction tests for genes using Drosophila are now being used so generally are conditions: 1) the system is useful for signal transduction genes; 2) the system can test neuronal differentiation potency; 3) the system uses a human gene, so as to be able to reflect a human function better than that reflected by a mouse; and 4) a mutation due to gene transfer is expressed exclusively in the compound eyes, so as to be able to avoid the disintegration of the experimental system due to death during development, unlike the case of knockout mice. Added herein is its usability as a gene breeding system. All the genes and substance groups do not function individually, but are present as substance groups or the functional protein assemblies that are involved in a certain function within a cell or an organism. Therefore, the precise capturing of functional dynamics of the whole pathway, in which the groups or the assemblies are involved, directly relates to the understanding of abnormalities in an organism, such as a disease. Drosophila flies can be genetically crossed with each other. Crossing with a group having a transgene or with a Drosophila group having a known genetic mutation can reveal a gene group involved in the transgene through the observation of individual mutations under physiological conditions.

[0008] Yamaguchi (one of the inventors) et al. have previously published a paper wherein it is shown that the gene transfer of a human cellular life span and cell death-determining factor p53 into the compound eye formation system of Drosophila enables the good reproduction of the cell death-inducing function at an individual level. Specifically, the process begins from the detection of the abnormal pathway of cells and tissue that have become cancerous, and the detection of causative genes involved in the pathway and the mutations. At the next step, the elucidation of substance groups to which these detection results are linked and the elucidation of the functions of the substance groups as an assembly are enabled in an individual model under physiological conditions. Only with such a series of analyses, disease control can be achieved.

[0009] The Bradeion gene-transferred Drosophila strain is a biosource, with which the cancer-specific correlation of a conventionally known gene and substance groups can be elucidated. This is carried out through a series of analyses concerning the elucidation of the signal transduction mechanism involved in cancer cell proliferation and division mediated by Bradeion, the detection of signalling substance groups within a cancer cell, and the elucidation of the dynamics thereof. Although Bradeion originally regulates the entry into the M-phase of the cell cycle during cell proliferation and division, it is observed in a human to show strong cell-specific expression and have a cell cycle-regulating function in colon cancer cells. Thus, it is assumed to be a key substance that enables the analysis of the abnormal homeostasis of cell groups that have been transformed to develop cancer. Furthermore, it is considered that Bradeion evidently functions by binding and associating with various substances participating in intracytoplasmic signal transduction.

[0010] The present invention can provide a new development of cancer control technology through analyses concerning the artificial re-transformation of cells and cell death induction by elucidating the signal transduction system that maintains cell division and proliferation within cancer cells, and provides the underlying data thereof.

[0011] Specifically, the results of these studies finally contribute to precise and cost-effective diagnosis, treatment and prophylaxis suited for individual gene type through cancer cell gene monitoring (diagnosis of canceration) and cancer cell division and proliferation control (gene therapy).

[0012] That is, the present invention is as described below.

[0013] (1) A Drosophila melanogaster strain, having the following properties:

[0014] (a) a human-derived Bradeion gene has been transferred in the strain to express the human-derived protein Bradeion in the compound eyes from the developmental period;

[0015] (b) the compound eyes show morphological abnormality due to the expression of Bradeion; and

[0016] (c) the morphological abnormality occurring in the compound eyes is multiplied according to the number of transferred Bradeion genes.

[0017] (2) The Drosophila melanogaster strain of (1), wherein the morphological abnormality in the compound eyes is referred to as “rough eye,” in which the cell cycles of each single eye are inconsistent.

[0018] (3)

[0019] (d) The Drosophila melanogaster strain of (1) or (2), which can be genetically crossed with other strains of Drosophila, which is able to transmit a trait introduced by the transferred Bradeion gene to the offspring, and which is able to inherit the inherited traits of other Drosophila strains to be crossed therewith.

[0020] The Bradeion gene can be obtained by purifying mRNA from human brain tissue, constructing a cDNA library and selecting the positive clone. A human Bradeion gene to be transferred into Drosophila includes DNA that can hybridize under stringent conditions to Bradeion DNA. Here, the term “stringent conditions” refers to conditions wherein hybridization occurs only when 90% or more, preferably 95% or more, and more preferably 97% or more homology is present between the Bradeion DNA sequence and the other sequence. Normally, under such conditions, hybridization occurs at approximately 5° C. to approximately 30° C., and preferably at approximately 10° C. to approximately 25° C., below the melting temperature of the complete hybrid. The stringent conditions are described in J. Sambrook et al., Molecular Cloning, A Laboratory Mannual, Second Edition, Cold Spring Harbor Laboratory Press (1989), and the conditions described therein can be employed. DNA capable of hybridizing under stringent conditions to the Bradeion DNA encodes a Bradeion analogue. Here, the analogue has characteristics substantially equivalent to those of human-derived Bradeion, and has an amino acid sequence derived from the amino acid sequence of human Bradeion by deletion, substitution or addition of at least one amino acid. The analogue preferably has 90% or more, preferably 95% or more, and more preferably 97% or more homology with Bradeion. Bradeion includes both a human a Bradeion and a human β Bradeion. The Bradeion gene can be obtained by a method disclosed in JP Patent Publication (Kokai) No. 2000-139470. In addition, DNA containing α Bradeion cDNA was deposited with the International Patent Organism Depositary, National Institute of Advanced Industrial Science and Technology (Chuo-6, 1-1-1, Higashi, Tsukuba-shi, Ibaraki, Japan) on Jul. 14, 1998, under FERM BP-6922. Furthermore, the α Bradeion gene and the β Bradeion gene were respectively deposited under accession Nos. E37353 and AB008753 or E37354 with the Gene Bank.

[0021] Moreover, the sequence of the a Bradeion gene is represented by SEQ ID NO: 1, and the sequence of the β Bradeion gene is represented by SEQ ID NO: 2. The entire sequence of SEQ ID NO: 1 or 2 may be transferred into Drosophila, or a portion ranging from positions 129 to 1943 of SEQ ID NO: 1 encoding a mature peptide (mat_peptide) of the a Bradeion protein, and a portion ranging from positions 129 to 1562 of SEQ ID NO: 2 encoding a mature peptide of the β Bradeion protein may be transferred into Drosophila.

[0022] The Bradeion gene can be transformed into Drosophila using, for example, a pUAST vector (Brand, A. H. and Perrimon, N. (1993) Development, 118, 401-415). The transferred Bradeion gene can be expressed specifically in the compound eye primordium using a GAL4-UAS target expression system (Brand, A. H. and Perrimon, N. (1993) Development, 118, 401-415.), thereby causing a morphological abnormality in the imaginal compound eyes. A fly having the Glass-GAL4 gene (optic primordium-specific Gal4 expression) is crossed with a fly having the UAS-Bradeion gene. The resulting Drosophila expresses Bradeion specifically in the optic primordium by transactivation of Bradeion, as shown in FIG. 1. The morphological abnormality resulting from Bradeion expression is referred to as “rough eye,” wherein the cell cycles of each single eye of the compound eyes are inconsistent. At this time, the morphological abnormality is enhanced by increasing the number of copies of the Bradeion gene to be transferred. Other biological characteristics of the Drosophila strain of the present invention are the same as those of normal Drosophila strains.

[0023] The Drosophila strain of the present invention can be crossed with other strains of Drosophila, can transmit the Bradeion gene transferred by crossing and genes of other strains used for crossing to the offspring, and can transmit a trait that is expressed by the transferred Bradeion gene and the inherited traits of other strains to the offspring.

[0024] The thus obtained Drosophila strain of the present invention can be stored and sent in the form of eggs.

[0025] A mutation that modifies the rough-eye phenotype resulting from the over-expression of Bradeion can be screened for by the following method. Specifically, approximately 200 Drosophila strains having deletion chromosomes (the sum of the chromosomal deletion regions of these strains corresponds to approximately 70% of the entire genome of Drosophila) are obtained from the Invertebrate Genetics Laboratory, Genetic Strain Research Center, National Institute of Genetics. Then, these strains are successively crossed with gene-transferred Drosophila strains showing a morphological abnormality in their compound eyes to transmit heterozygous deletion chromosomes to the offspring. Screening is then performed for strains wherein the morphological abnormality in the compound eyes is suppressed or enhanced. Then, lethal mutant strains (available from the genome projects in the U.S. and Europe) in which P-element has been inserted within the chromosomal region showing suppression or enhancement due to deletion (which is shown as a result of these crossing experiments) are collected, and then similar crossing experiments can be conducted.

[0026] Furthermore, a novel molecular target of a therapeutic agent for diagnosing cancer using Bradeion as an indicator can also be searched for by the following method. Specifically, the above lethal mutant strains into which P-element has been inserted showing the suppressed or enhanced phenotype are obtained, and then genes that are inactivated by P-element insertion are cloned by the P-element plasmid rescue method. The partial nucleotide sequences of the cloned genes are determined, the gene products thereof are identified by searching the database, and then human homologues thereof are cloned using a standard method. In addition, analysis is made for the genetic interaction between the thus obtained lethal mutant strains into which P-element has been inserted and the mutant strains of a known gene for regulating higher order chromosome structure, a cell cycle-related gene or an apoptosis-related gene.

[0027] Moreover, a candidate for a novel anticancer agent can be searched for by screening for an agent that suppresses the morphological abnormality exhibited by the thus established gene-transferred Drosophila.

[0028] The present invention will be described more specifically by the following examples. These examples are not intended to limit the present invention.

BRIEF DESCRIPTION OF THE DRAWINGS

[0029]FIG. 1 is a schematic view showing a method for transferring the Bradeion gene into Drosophila so that the gene can be expressed.

[0030]FIG. 2 contains photographs showing the normally expressed imaginal Drosophila compound eyes, and the imaginal compound eyes exhibiting morphological abnormality in the compound eyes (rough eye).

[0031]FIG. 3 contains photographs showing, for example the imaginal Drosophila compound eyes exhibiting morphological abnormality in the compound eyes (rough eye).

BEST MODE OF CARRYING OUT THE INVENTION EXAMPLE 1

[0032] Bradeion cDNA was ligated to Xho I-EcoR I (blunt-ended) cleavage site located downstream of a promoter having a transcription factor GAL4 binding sequence of a pUAST vector (Brand, A. H. and Perrimon, N. (1993). Development, 118, 401-415), thereby obtaining a recombinant plasmid DNA (pUAST-Bradeion). The DNA was transferred into Escherichia coli for transformation, and then the bacteria were grown (FIG. 1).

[0033] pUAST-Bradeion DNA was purified using a Qiagen column, and then injected in a minute amount into the fertilized eggs of a Drosophila strain, which is white gene (−) and has a transposase gene (Spradling, A. C. (1986). Drosophila: a practical approach. Roberts, D. B. (ed.). IRL Press: Oxford, pp. 175-197), and then a trasformant that was rescued with a white gene marker present within the pUAST-Bradeion DNA was selected (Robertson, H. M., Preston, C. R., Philips, R. W., Johnson-Schlitz, D. M., Benz, W. K. and Engels, W. R. (1988). Genetics, 118, 461-470). The thus established strains are summarized in Table 1 below. TABLE 1 P-element plasmid Strain Chromosomal linkage pUAS-Bradeion  4 II 19 X 25 III 27 II 38 II 46 III 54 II

[0034] The compound eye pimordium-specific over-expression of Bradeion using the GAL4-UAS target expression system (Brand, A. H. and Perrimon, N. (1993). Development, 118, 401-415) causes a morphological abnormality in the imaginal compound eyes (rough eye phenotype) (FIG. 2B) (FIG. 2A shows a control). The morphological abnormality was further enhanced by increasing the number of copies of a UAS-Bradeion gene (FIG. 2C). These morphological abnormalities were suppressed by the co-expression of Drosophila anti-apoptosis proteins DIAP1 (FIG. 3B) and DIAP2 (FIG. 3C), or Baculovirus anti-apoptosis protein P35 (FIG. 3D) in the compound eye primordium. Based on these results, it is considered that the over-expression of Bradeion induces apoptosis in the cells of the compound eye primordium, so as to cause a morphological abnormality in the imaginal compound eyes.

INDUSTRIAL APPLICABILITY

[0035] By the use of the Bradeion gene-transferred Drosophila strain of the present invention, precise and cost-effective diagnosis, treatment and prophylaxis suited for an individual gene type can be finally achieved through cancer cell gene monitoring (diagnosis of canceration) and the regulation of cancer cell division and proliferation (gene therapy).

1 2 1 2274 DNA Homo sapiens mat_peptide (129)...(1943) 1 gaaaggagca agccaggaag ccagacaaca acagcatcaa aacaaggctg tttctgtgtg 60 tgaggaactt tgcctgggag ataaaattag acctagagct ttctgacagg gagtctgaag 120 cgtgggacat ggaccgttca ctgggatggc aagggaattc tgtccctgag gacaggactg 180 aacctgggat caaccgtttc ctggaggaca ccacggatga tggagaactg agcaagttcg 240 tgaaggattt ctcaggaaat gcgagctgcc acccaccaga ggctaagacc tgggcatcca 300 ggccccaagt cccggagcca aggccccagg ccccggacct ctatgatgat gacctggagt 360 tcagaccccc ctcgcggccc cagtcctctg acaaccagca gtacttctgt gccccagccc 420 ctctcagccc atctgccagg ccccgcagcc catgggggga gcttgatccc tatgattcct 480 ctgaggtaga gcctccagcc ctgcctttgc ctttcagtgg gctgctgcag gaagaccggg 540 ggcagggagc aggaatgtgt gtgtgtgtgt gtgtgtgtgt gtgtgtgtgt gtgtttgtgt 600 gtgtgtgtat ctgggaccca tttcagtcct gtgtcagccc tagctccaaa atatctgccc 660 ccaagggcac tggaaatttg cagtttcagc aagggcagga ggcccagctg gtggcctcag 720 atgggaactc acagaagtct ggcactgctt ttttaaggct ggggcaaagg cctgaaaggg 780 agagaagatt ggcgctgggt gccggggccc ctttggctcc tcaccgtgat gcattctgcc 840 ttcctgtcta ctacgatgac aaggagtatg tgggctttgc aaccctcccc aaccaagtcc 900 accgaaagtc cgtgaagaaa ggctttgact ttaccctcat ggtggcagga gagtctggcc 960 tgggcaaatc cacacttgtc aatagcctct tcctcactga tctgtaccgg gaccggaaac 1020 ttcttggtgc tgaagaaagg atcatgcaaa ctgtggagat cactaagcat gcagtggaca 1080 tagaaaaaaa aggtgtgagg ctgcggctca ccattgtgga cacaccaagt tttggggatg 1140 cagtcaacaa cacagagtgt atgtctgact ggaagcctgt ggcagaatac attgatcagc 1200 agtttgagca gtatttccga gacgagagtg gcctgaaccg aaagaacatc caagacaaca 1260 gggtgcactg ctgcctgtac ttcatctcac ccttcggcca tgggctccgg ccattggatg 1320 ttgaattcat gaaggccctg catcagcggg tcaacatcgt gcctatcctg gctaaggcag 1380 acacactgac acctcccgaa gtggaccaca agaaacgcaa aatccgggag gagattgagc 1440 attttggaat caagatctat caattcccag actgtgactc tgatgaggat gaggacttca 1500 aattgcagga ccaagcccta aaggaaagca tcccatttgc agtaattggc agcaacactg 1560 tagtagaggc cagagggcgg cgagttcggg gtcgactcta cccctggggc atcgtggaag 1620 tggaaaaccc agggcactgc gactttgtga agctgaggac aatgctggta cgtacccaca 1680 tgcaggacct gaaggatgtg acacgggaga cacattatga gaactaccgg gcacagtgca 1740 tccagagcat gacccgcctg gtggtgaatg aacggaatcg caagtatgac cagaagccag 1800 gacaaagctg gcagggggag atcccaagcc tagccttggg tgagaccaag ccctactttt 1860 gttcttctat aggccctggg ctcaatctaa gcgggtgctg gggtcctcct cgccttatca 1920 acccttttct ccctttagca aactgactcg ggaaagtggt accgacttcc ccatccctgc 1980 tgtcccacca gggacagatc cagaaactga gaagcttatc ccagagaaag attaggagct 2040 gcggcggata cacgagatac tacaccaaat accaaaacag ataaaggaga actatttact 2100 ggctttcagc cctggatatt taaatctcct cctcttcttc ctgtccatgc cggcccctcc 2160 cagcaccagc tctgctcagg ccccttcagc tactgccact tcgccttaca tccctgctga 2220 ctgcccagag actcagagga aataaagttt aataaatctg taggtggctt ctgg 2274 2 1735 DNA Homo sapiens mat_peptide (129)...(1562) 2 gaaaggagca agccaggaag ccagacaaca acagcatcaa aacaaggctg tttctgtgtg 60 tgaggaactt tgcctgggag ataaaattag acctagagct ttctgacagg gagtctgaag 120 cgtgggacat ggaccgttca ctgggatggc aagggaattc tgtccctgag gacaggactg 180 aagctgggat caagcgtttc ctggaggaca ccacggatga tggagaactg agcaagttcg 240 tgaaggattt ctcaggaaat gcgagctgcc acccaccaga ggctaagacc tgggcatcca 300 ggccccaagt cccggagcca aggccccagg ccccggacct ctatgatgat gacctggagt 360 tcagaccccc ctcgcggccc cagtcctctg acaaccagca gtacttctgt gccccagccc 420 ctctcagccc atctgccagg ccccgcagcc catggggcaa gcttgatccc tatgattcct 480 ctgaggatga caaggagtat gtgggctttg caaccctccc caaccaagtc caccgaaagt 540 ccgtgaagaa aggctttgac tttaccctca tggtggcagg agagtctggc ctgggcaaat 600 ccacacttgt caatagcctc ttcctcactg atctgtaccg ggaccggaaa cttcttggtg 660 ctgaagagag gatcatgcaa actgtggaga tcactaagca tgcagtggac atagaagaga 720 agggtgtgag gctgcggctc accattgtgg acacaccagg ttttggggat gcagtcaaca 780 acacagagtg ctggaagcct gtggcagaat acattgatca gcagtttgag cagtatttcc 840 gagacgagag tggcctgaac cgaaagaaca tccaagacaa cagggtgcac tgctgcctgt 900 acttcatctc acccttcggc catgggctcc ggccattgga tgttgaattc atgaaggccc 960 tgcatcagcg ggtcaacatc gtgcctatcc tggctaaggc agacacactg acacctcccg 1020 aagtggacca caagaaacgc aaaatccggg aggagattga gcattttgga atcaagatct 1080 atcaattccc agactgtgac tctgatgagg atgaggactt caaattgcag gaccaagccc 1140 taaaggaaag catcccattt gcagtaattg gcagcaacac tgtagtagag gccagagggc 1200 ggcgagttcg gggtcgactc tacccctggg gcatcgtgga agtggaaaac ccagggcact 1260 gcgactttgt gaagctgagg acaatgctgg tacgtaccca catgcaggac ctgaaggatg 1320 tgacacggga gacacattat gagaactacc gggcacagtg catccagagc atgacccgcc 1380 tggtggtgaa ggaacggaat cgcaacaaac tgactcggga aagtggtacc gacttcccca 1440 tccctgctgt cccaccaggg acagatccag aaactgagaa gcttatccga gagaaagatg 1500 aggagctgcg gcggatgcag gagatgctac acaaaataca aaaacagatg aaggagaact 1560 attaactggc tttcagccct ggatatttaa atctcctcct cttcttcctg tccatgccgg 1620 cccctcccag caccagctct gctcaggccc cttcagctac tgccacttcg cctaacatcc 1680 ctgctgactg cccagagact cagaggaaat aaagtttaat aaatctgtag gtggc 1735 

What is claimed is:
 1. A Drosophila melanogaster strain, having the following properties: (a) a human-derived Bradeion gene has been transferred in the strain to express the human-derived protein Bradeion in the compound eyes from the developmental period; (b) the compound eyes show morphological abnormality due to the expression of Bradeion; and (c) the morphological abnormality occurring in the compound eyes is multiplied according to the number of transferred Bradeion genes.
 2. The Drosophila melanogaster strain of claim 1, wherein the morphological abnormality in the compound eyes is referred to as “rough eye,” in which the cell cycles of each single eye are inconsistent.
 3. (d) The Drosophila melanogaster strain of claim 1 or 2, which can be genetically crossed with other strains of Drosophila, which is able to transmit a trait introduced by the transferred Bradeion gene to the offspring, and which is able to inherit the inherited traits of other Drosophila strains to be crossed therewith. 